Description

Ziprasidone Mesilate is the mesylate salt form of ziprasidone, a potent atypical antipsychotic agent. This high-purity active pharmaceutical ingredient (API) is critical for ensuring the efficacy and safety of finished pharmaceutical formulations. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of antipsychotic medications for the treatment of schizophrenia and bipolar disorder.

Application

• Pharmaceutical API: Primary use as the active ingredient in the manufacture of antipsychotic drug products, including tablets and capsules.
• Reference Standard: Serves as a certified reference material (CRM) for quality control and analytical method development in pharmaceutical laboratories.
• Research & Development: Used in preclinical and clinical studies to investigate the pharmacology and therapeutic potential of ziprasidone.
• Formulation Development: Key component in the development of novel drug delivery systems and dosage forms to improve patient compliance.

Basic Information

Product Name	Ziprasidone Mesilate
CAS No.	199191-69-0
Molecular Formula	C22H21ClN4OS • CH4O3S
Molecular Weight	509.00 g/mol
Synonyms	Ziprasidone Methanesulfonate; Ziprasidone Mesylate; 5-[2-[4-(1,2-Benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-2H-indol-2-one Methanesulfonate; Geodon Mesylate; Zeldox Mesylate; CP-88059-1
EINECS	Contact for details

Quality Control

Our Ziprasidone Mesilate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency, aligning with ICH guidelines. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 1.0% Any individual impurity ≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.